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临床试验/NL-OMON48466
NL-OMON48466已完成不适用

Determining the fingerprint of endotoxin tolerance - 100LPS study

Radboud Universitair Medisch Centrum0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
100

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • * Written informed consent
  • * Age *18 and *35 yrs
  • * Healthy (as confirmed by medical history, physical examination,
  • electrocardiography, laboratory tests)

排除标准

  • * Pregnancy (confirmed by negative result of pregnancy tests prior to both
  • endotoxin challenges)
  • * Use of any medication
  • * History or signs of atopic syndrome (asthma, rhinitis with medication and/or
  • * Known anaphylaxis or hypersensitivity to the non-investigational products or
  • their excipi-ents.
  • * History or signs of hematological disease:
  • * Thrombocytopenia (<150*10^9/ml) or anemia (for males: hemoglobin < 8.0 mmol/L
  • and for females: hemoglobin < 7.4 mmol/L)
  • * Abnormalities in leukocyte differential counts
  • * History, signs or symptoms of cardiovascular disease, in particular:
  • * Previous spontaneous vagal collapse
  • * History of atrial or ventricular arrhythmia
  • * Cardiac conduction abnormalities on the ECG consisting of a 2nd degree
  • atrioventricular block or a complete left bundle branch block
  • * Hypertension (defined as RR systolic > 160 or RR diastolic > 90)
  • * Hypotension (defined as RR systolic < 100 or RR diastolic < 50)
  • * Renal impairment (defined as plasma creatinine >120 *mol/l)
  • * Liver enzyme abnormalities (above 2x the upper limit of normal)
  • * Medical history of any disease associated with immune deficiency
  • * Signs of infection (CRP > 20 mg/L, WBC > 12x109/L or < 4 x109/L)
  • * Clinically significant acute illness, including infections, within 1 month of
  • the first endotoxin challenge
  • * Previous (participation in a study with) endotoxin (LPS) administration
  • * Any vaccination within 3 months within of the first endotoxin challenge
  • * Participation in a drug trial or donation of blood within 3 months prior to
  • first endotoxin challenge
  • * Recent hospital admission or surgery with general anesthesia within 3 months
  • prior to first endotoxin challenge
  • * Use of recreational drugs within 1 month of the first endotoxin challenge
  • * Inability to personally provide written informed consent (e.g. for linguistic
  • or mental rea-sons) and/or take part in the study.

研究者

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